Validation Engineering Specialist II – Equipment Engineering

Seeking a Validation Engineering Specialist II to support equipment, facilities, and process validation in a GMP-regulated environment. This role involves leading commissioning and qualification activities, preparing IQ/OQ/PQ protocols and reports, reviewing vendor documentation, supporting audits and CAPAs, and collaborating with clients, project managers, and stakeholders.

A minimum of 3 years' experience in validation, process engineering, or quality in pharma or biotech is required.